NCBI
dbSNP

dbVar ClinVar GaP PubMed Nucleotide Protein
Search small variations in dbSNP or large structural variations in dbVar
transparent GIF
Spacer gif
Have a question about dbSNP? Try searching the SNP FAQ Archive!

Spacer gif
Submitted SNP(ss) Details: ss168876402           
Submitter
HandleILLUMINA
Submitter SNP IDHumanCNV370-Quadv3_C_cnvi0000027-126_B_R_1514265407
RefSNP(rs#)rs56384684
Submitted Batch IDHumanCNV370-Quadv3_C
Submitted DateOct 01, 2009
Publication CitedN.D.
First entry to dbSNPOct 1 2009 12:00:00:000AM
Assay
SpeciesHomo sapiens
Molecular
Type
Genomic
MethodILLUMINA-CUSTOMERIZED-CHIP
Ascertainment Samplesize270
PopulationN.D.
Allele
Observed AlleleC/T
Ancestral AlleleN.D.
Allele OriginN/A
SNP ClassSNV
CpG CodeN.D.
Validation
Validation StatusNot Validated
HWE Goodness of Fitnot applicable
Variation
Frequency SubmissionN.D.
Genotype SummaryN.D.
Genotype SubmissionN.D.
HaplotypeN.D.

  Fasta sequence   (Legend) back to top
>gnl|dbSNP|ss168876402|allelePos=59|len=111|taxid=9606|alleles='C/T'|mol=Genomic
 AGACTGGTCT TGAACTCCAG GCTGGTCTTG AACTCCAAGA GGCCTTGAGT GCTGGGCT
 Y
 AAGCAATCCA CCTGCTTCAG CCTCCCAAAG TGCTGGGATT ACAGGCATGA GC

  Submitted Frequency for ss168876402 back to top
There is no frequency submission for ss168876402.


  dbSNP summary of Genotypes for ss168876402 back to top
No sufficient data to compute Hardy-weinberg probability for ss168876402.


  Submitted individual genotype for ss168876402 back to top
There is no individual genotype data for ss168876402.